CL2016003301A1 - Substituted amino- (pyridine-4-carboxylic acid) derivative compounds, histone demethylase inhibitors; pharmaceutical composition, comprising them, useful in the treatment of cancer, such as prostate, breast, bladder, lung and / or melanoma cancer. - Google Patents
Substituted amino- (pyridine-4-carboxylic acid) derivative compounds, histone demethylase inhibitors; pharmaceutical composition, comprising them, useful in the treatment of cancer, such as prostate, breast, bladder, lung and / or melanoma cancer.Info
- Publication number
- CL2016003301A1 CL2016003301A1 CL2016003301A CL2016003301A CL2016003301A1 CL 2016003301 A1 CL2016003301 A1 CL 2016003301A1 CL 2016003301 A CL2016003301 A CL 2016003301A CL 2016003301 A CL2016003301 A CL 2016003301A CL 2016003301 A1 CL2016003301 A1 CL 2016003301A1
- Authority
- CL
- Chile
- Prior art keywords
- cancer
- prostate
- bladder
- breast
- lung
- Prior art date
Links
- 108010074870 Histone Demethylases Chemical class 0.000 title abstract 3
- 102000008157 Histone Demethylases Human genes 0.000 title abstract 3
- 206010028980 Neoplasm Diseases 0.000 title 2
- 201000011510 cancer Diseases 0.000 title 2
- -1 amino- (pyridine-4-carboxylic acid) derivative compounds Chemical class 0.000 title 1
- 210000000481 breast Anatomy 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 210000004072 lung Anatomy 0.000 title 1
- 201000001441 melanoma Diseases 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 210000002307 prostate Anatomy 0.000 title 1
- 210000003932 urinary bladder Anatomy 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 4
- 101001025971 Homo sapiens Lysine-specific demethylase 6B Proteins 0.000 abstract 2
- 102100037461 Lysine-specific demethylase 6B Human genes 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 238000000338 in vitro Methods 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4433—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with oxygen as a ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/79—Acids; Esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Enzymes And Modification Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
Abstract
La presente invención se refiere a un compuesto, o un estereoisómero o sal farmacéuticamente aceptable del mismo, que tiene la estructura de la fórmula (II): Además, la invención divulga el compuesto, o sal farmacéuticamente aceptable del mismo, de la reivindicación 1 de fórmula (IIa): Además, la presente invención divulga un método in vitro para inhibir una enzima JMJD3 de histona desmetilasa que comprende poner en contacto la enzima histona desmetilasa JMJD3 con un compuesto de fórmula (II), la presente invención divulga el uso del compuesto de fórmula (II).The present invention relates to a compound, or a stereoisomer or pharmaceutically acceptable salt thereof, having the structure of formula (II): Furthermore, the invention discloses the compound, or pharmaceutically acceptable salt thereof, of claim 1 of Formula (IIa): Furthermore, the present invention discloses an in vitro method for inhibiting a histone demethylase enzyme JMJD3 comprising contacting the histone demethylase enzyme JMJD3 with a compound of formula (II), the present invention discloses the use of the compound of formula (II).
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462017201P | 2014-06-25 | 2014-06-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2016003301A1 true CL2016003301A1 (en) | 2021-03-05 |
Family
ID=54929774
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2016003301A CL2016003301A1 (en) | 2014-06-25 | 2016-12-22 | Substituted amino- (pyridine-4-carboxylic acid) derivative compounds, histone demethylase inhibitors; pharmaceutical composition, comprising them, useful in the treatment of cancer, such as prostate, breast, bladder, lung and / or melanoma cancer. |
Country Status (29)
| Country | Link |
|---|---|
| US (7) | US10385047B2 (en) |
| EP (3) | EP3741749A1 (en) |
| JP (1) | JP6521535B2 (en) |
| KR (1) | KR102591897B1 (en) |
| CN (2) | CN106660982B (en) |
| AR (1) | AR100997A1 (en) |
| AU (1) | AU2015279719B2 (en) |
| BR (1) | BR112016030367A2 (en) |
| CA (1) | CA2953437C (en) |
| CL (1) | CL2016003301A1 (en) |
| CO (1) | CO2017000359A2 (en) |
| CY (1) | CY1123906T1 (en) |
| DK (1) | DK3160952T3 (en) |
| EA (1) | EA031200B1 (en) |
| EC (1) | ECSP17004931A (en) |
| ES (1) | ES2862648T3 (en) |
| HR (1) | HRP20210299T1 (en) |
| HU (1) | HUE053876T2 (en) |
| IL (1) | IL249629A0 (en) |
| LT (1) | LT3160952T (en) |
| MX (1) | MX375219B (en) |
| NZ (1) | NZ728120A (en) |
| PL (1) | PL3160952T3 (en) |
| PT (1) | PT3160952T (en) |
| SA (1) | SA516380585B1 (en) |
| SG (1) | SG11201610813TA (en) |
| SI (1) | SI3160952T1 (en) |
| TW (2) | TWI715533B (en) |
| WO (1) | WO2015200709A1 (en) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HK1210611A1 (en) | 2012-12-21 | 2016-04-29 | Quanticel Pharmaceuticals Inc | Histone demethylase inhibitors |
| AU2015279719B2 (en) | 2014-06-25 | 2019-03-21 | Celgene Quanticel Research, Inc. | Histone demethylase inhibitors |
| US10030017B2 (en) | 2014-09-17 | 2018-07-24 | Celgene Quanticel Research, Inc. | Histone demethylase inhibitors |
| KR20170048591A (en) | 2014-09-17 | 2017-05-08 | 셀젠 콴티셀 리서치, 인크. | Histone demethylase inhibitors |
| CN108698997A (en) | 2015-12-28 | 2018-10-23 | 赛尔基因昆蒂赛尔研究公司 | Histone demethylase inhibitors |
| ES2921009T3 (en) * | 2016-03-15 | 2022-08-16 | Celgene Quanticel Res Inc | Histone demethylase inhibitors |
| US10150754B2 (en) | 2016-04-19 | 2018-12-11 | Celgene Quanticel Research, Inc. | Histone demethylase inhibitors |
| WO2018183370A2 (en) * | 2017-03-30 | 2018-10-04 | Albert-Ludwigs-University Freiburg | Kdm4 inhibitors |
| CN109825551B (en) * | 2019-02-21 | 2022-08-02 | 深圳大学 | A method for evaluating histone lysine demethyltransferase activity |
| CN111679072B (en) * | 2020-06-15 | 2022-04-29 | 温州医科大学 | Application of KDM6B protein in breast cancer prognosis assessment kits and diagnostic kits |
| WO2022217100A1 (en) * | 2021-04-09 | 2022-10-13 | Tachyon Therapeutics, Inc. | Treatment of cancer with kdm4 inhibitors |
| EP4387961A1 (en) * | 2021-08-18 | 2024-06-26 | Celgene Corporation | Process for preparing histone demethylase inhibitors |
| AU2022419374A1 (en) * | 2021-12-23 | 2024-07-18 | Tachyon Therapeutics, Inc. | Pharmaceutical formulations comprising 3-({[(4r)-7-{methyl[4-(propan-2-yl)phenyl]amino}-3,4-dihydro-2h-l-benzopyran-4-yl]methyl}amino)pyridine-4-carboxylic acid |
| AR129578A1 (en) | 2022-06-10 | 2024-09-11 | Forward Therapeutics Inc | MODULATORS OF TNF-a ACTIVITY |
| US20250241905A1 (en) * | 2022-06-23 | 2025-07-31 | The Cleveland Clinic Foundation | 3-beta-hsd1 inhibitors and compositions and uses thereof |
| CN120225189A (en) * | 2022-09-21 | 2025-06-27 | 细胞基因公司 | Crystalline form of histone demethylase inhibitor 3-({[(4R)-7-{methyl[4-(propan-2-yl)phenyl]amino}-3,4-dihydro-2H-1-benzopyran-4-yl]methyl}amino)pyridine-4-carboxylic acid L-lysine salt |
| CN115974647B (en) * | 2022-12-05 | 2024-09-03 | 江苏宏邦化工科技有限公司 | Method for preparing cola amyl alcohol by taking tetrahydro-4-methyl-2-phenyl-2H-pyran-4-alcohol as raw material |
| WO2025085527A1 (en) * | 2023-10-16 | 2025-04-24 | The Cleveland Clinic Foundation | 3βHSD1 INHIBITORS AND COMPOSITIONS AND USES THEREOF |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2465978C (en) * | 2001-09-14 | 2015-04-07 | Soon Hyung Woo | Inhibitors of histone deacetylase |
| UA89035C2 (en) | 2003-12-03 | 2009-12-25 | Лео Фарма А/С | Hydroxamic acid esters and pharmaceutical use thereof |
| DE102004039876A1 (en) | 2004-06-23 | 2006-01-26 | Lanxess Deutschland Gmbh | Preparation of fluorinated 1,3-benzodioxanes |
| TW200808793A (en) | 2006-03-07 | 2008-02-16 | Smithkline Beecham Corp | Prolyl hydroxylase inhibitors |
| JP5554988B2 (en) * | 2006-04-07 | 2014-07-23 | メチルジーン インコーポレイテッド | Inhibitors of histone deacetylase |
| US7898712B2 (en) | 2008-06-27 | 2011-03-01 | Lockheed Martin Corporation | Risley integrated steering module |
| GB201112607D0 (en) | 2011-07-22 | 2011-09-07 | Glaxo Group Ltd | Novel compounds |
| JP6240063B2 (en) * | 2011-04-28 | 2017-11-29 | ザ ブロード インスティテュート， インコーポレイテッド | Histone deacetylase inhibitor |
| WO2013143597A1 (en) * | 2012-03-29 | 2013-10-03 | Glaxo Group Limited | Demethylase enzymes inhibitors |
| US20140162266A1 (en) | 2012-12-05 | 2014-06-12 | Bio-Rad Laboratories, Inc. | Methods for polymerase chain reaction copy number variation assays |
| ES2834959T3 (en) | 2012-12-06 | 2021-06-21 | Celgene Quanticel Res Inc | Histone demethylase inhibitors |
| US9617242B2 (en) * | 2012-12-19 | 2017-04-11 | Celgene Quanticel Research, Inc. | Histone demethylase inhibitors |
| HK1210611A1 (en) * | 2012-12-21 | 2016-04-29 | Quanticel Pharmaceuticals Inc | Histone demethylase inhibitors |
| AU2015279719B2 (en) | 2014-06-25 | 2019-03-21 | Celgene Quanticel Research, Inc. | Histone demethylase inhibitors |
| WO2018183370A2 (en) * | 2017-03-30 | 2018-10-04 | Albert-Ludwigs-University Freiburg | Kdm4 inhibitors |
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2015
- 2015-06-25 AU AU2015279719A patent/AU2015279719B2/en active Active
- 2015-06-25 NZ NZ728120A patent/NZ728120A/en unknown
- 2015-06-25 SI SI201531524T patent/SI3160952T1/en unknown
- 2015-06-25 WO PCT/US2015/037812 patent/WO2015200709A1/en not_active Ceased
- 2015-06-25 HU HUE15811523A patent/HUE053876T2/en unknown
- 2015-06-25 TW TW104120633A patent/TWI715533B/en active
- 2015-06-25 PT PT158115238T patent/PT3160952T/en unknown
- 2015-06-25 HR HRP20210299TT patent/HRP20210299T1/en unknown
- 2015-06-25 EA EA201692483A patent/EA031200B1/en unknown
- 2015-06-25 LT LTEP15811523.8T patent/LT3160952T/en unknown
- 2015-06-25 EP EP20184106.1A patent/EP3741749A1/en active Pending
- 2015-06-25 EP EP20184107.9A patent/EP3738960A1/en not_active Withdrawn
- 2015-06-25 EP EP15811523.8A patent/EP3160952B1/en active Active
- 2015-06-25 TW TW109143458A patent/TWI758004B/en active
- 2015-06-25 AR ARP150102042A patent/AR100997A1/en not_active Application Discontinuation
- 2015-06-25 SG SG11201610813TA patent/SG11201610813TA/en unknown
- 2015-06-25 US US15/321,702 patent/US10385047B2/en active Active
- 2015-06-25 DK DK15811523.8T patent/DK3160952T3/en active
- 2015-06-25 JP JP2016574454A patent/JP6521535B2/en active Active
- 2015-06-25 CN CN201580045921.2A patent/CN106660982B/en active Active
- 2015-06-25 MX MX2016017407A patent/MX375219B/en active IP Right Grant
- 2015-06-25 CA CA2953437A patent/CA2953437C/en active Active
- 2015-06-25 PL PL15811523T patent/PL3160952T3/en unknown
- 2015-06-25 KR KR1020177002223A patent/KR102591897B1/en active Active
- 2015-06-25 BR BR112016030367A patent/BR112016030367A2/en not_active Application Discontinuation
- 2015-06-25 ES ES15811523T patent/ES2862648T3/en active Active
- 2015-06-25 CN CN202010813617.0A patent/CN111909083B/en active Active
- 2015-06-25 US US14/751,007 patent/US9242968B2/en active Active
- 2015-12-09 US US14/963,754 patent/US9447046B2/en active Active
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2016
- 2016-07-26 US US15/220,118 patent/US9586902B2/en active Active
- 2016-12-18 IL IL249629A patent/IL249629A0/en unknown
- 2016-12-22 CL CL2016003301A patent/CL2016003301A1/en unknown
- 2016-12-22 SA SA516380585A patent/SA516380585B1/en unknown
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2017
- 2017-01-09 US US15/402,100 patent/US9815828B2/en active Active
- 2017-01-16 CO CONC2017/0000359A patent/CO2017000359A2/en unknown
- 2017-01-24 EC ECIEPI20174931A patent/ECSP17004931A/en unknown
- 2017-10-24 US US15/792,570 patent/US9994561B2/en active Active
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2018
- 2018-05-04 US US15/971,749 patent/US10106534B2/en active Active
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2021
- 2021-03-01 CY CY20211100169T patent/CY1123906T1/en unknown
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